Levothyroxine Sodium Tablets Recall by Accord Healthcare
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Accord Healthcare Inc. is recalling certain lots of Levothyroxine Sodium Tablets, USP 200 mcg due to subpotent drug classification.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on September 7, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened
Accord Healthcare, Inc. initiated a voluntary recall of Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg) classified as Class II by the FDA for subpotent drug.
Which Products Are Affected
The recall affects Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg) packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-count bottles (NDC 16729-457-17). Affected lots include a) Lot # D2402430, D2402431 (Exp. 10/31/2026) and b) Lot # D2402432 (Exp. 10/31/2026), D2500180 (Exp. 12/31/2026). The products were distributed nationwide within the United States. Recall number D-0785-2026.
What You Should Do
Consumers with questions should contact the recalling firm, Accord Healthcare, Inc.
Why This Matters
This Class II recall involves a subpotent drug distributed nationwide.
Source
FDA recall D-0785-2026 - Accord Healthcare, Inc., Raleigh, NC.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (905 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.